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Test Code ACOGFRX ACOG Panel with Fragile X

Performing Laboratory

Counsyl, Inc.

Methodology

The Counsyl Test-Genotyping

Includes:

Bloom syndrome

Canavan disease

Cystic Fibrosis

Familial dysautonomia

Fanconi anemia type C

Gaucher disease

Hb beta chain-related hemoglobinopathy

Hexosaminidase A deficiency

Mucolipidosis IV

Niemann-Pick disease, SMPD1-associated

Spinal muscular atrophy

 

Specimen Required

Container/Tube:  Lavender top tube(s)

Specimen: Whole Blood 3 ml's

Transport Temperature: Room Temperature

 

Note:

Requires Ethnicity (required for interpretation)

 Choices are:

  1. Northern European (British, German)
  2. Southern European (Italian, Greek)
  3. French Canadian
  4. Ashkenazi Jewish
  5. Finnish
  6. Other/Mixed Caucasian
  7. East Asian (Chinese, Japanese)
  8. South Asian (Indian, Pakistani)
  9. Southeast Asian (Filipino, Vietnamese)
  10. African or African American
  11. Hispanic
  12. Middle Eastern
  13. Native American
  14. Pacific Islander
  15. Unknown

Reference Values

See Report

Test Classification and CPT Coding

 

81200

Canavan

81209

Bloom Syndrome

81220

Cystic Fibrosis

81242

Fanconi Anemia

81251

Gaucher Disease

81255

Tay Sachs

81260

Familial Dysautonomia

81290

Mucolipidosis IV

81330

Niemann-Pick Disease

81332

Alpha 1 Antitrypsin Deficiency

81400

SMN1

81401

HBB (Hemoglobin, Beta)

 

Computer Interface Code

PDM # 1559067